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Postion:Product Catalog >Organic Chemistry>Organometallic compounds>Organolithium>Methyllithium
Methyllithium
  • Methyllithium
  • Methyllithium
  • Methyllithium
  • Methyllithium
  • Methyllithium

Methyllithium NEW

Price Get Latest Price
Package 25KG
Min. Order: 1KG
Supply Ability: 50000KG/month
Update Time: 2023-08-18

Product Details

Product Name: Methyllithium CAS No.: 917-54-4
EC-No.: 213-026-4 Min. Order: 1KG
Purity: 99% Supply Ability: 50000KG/month
Release date: 2023/08/18

CAS:917-54-4
MF:CH3Li
MW:21.98
EINECS:213-026-4
Product Categories:metal alkyl;Classes of Metal Compounds;Li (Lithium) Compounds;Typical Metal Compounds;25mL Sure/Seal Reagents;Alkyl;Chemical Synthesis;Organic Bases;Organolithium;Organometallic Reagents;Synthetic Reagents
Mol File:917-54-4.mol
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Methyllithium Chemical Properties
Melting point 70-71℃
Boiling point 88℃
density 0.85 g/mL at 20 °C
vapor density 3 (vs air)
Fp 5 °F
storage temp. 2-8°C
form Solution
Specific Gravity0.83
color Colorless to yellow
Water Solubility Reacts with water.
Sensitive Air & Moisture Sensitive
Hydrolytic Sensitivity9: reacts extremely rapidly with atmospheric moisture - may be pyrophoric - glove box or sealed system required
BRN 3587162
Exposure limitsACGIH: TWA 400 ppm; STEL 500 ppm
OSHA: TWA 400 ppm(1200 mg/m3)
NIOSH: IDLH 1900 ppm
CAS DataBase Reference917-54-4(CAS DataBase Reference)
EPA Substance Registry SystemLithium, methyl- (917-54-4)

Methyllithium Usage And Synthesis
Chemical Properties

Methyllithium is a colorless to yellowish solution, It is insoluble in hydrocarbon solvents although propyllithium and the higher homologues are miscible in hydrocarbons. Methyllithium is soluble in diethyl ether to about 6% by weight at room temperature (with or without lithium bromide) and is a little less soluble in tetrahydrofuran. Cooling of these solutions produces clear, colorless crystals of methyllithium etherate. Methyllithium is stable to about 200°C, at which temperature it disproportionates to dilithiomethane and methane.
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UsesThere are no significant industrial uses of methyllithium, but it is widely used in the laboratory in Grignard type reactions.
Methyllithium is an organolithium reagent mainly used for deprotonation and as a source of methyl anion. It is a strong base and a strong nucleophile.
UsesMethyllithium lithium bromide complex solution (MeLi.LiBr) can be used as a methylating agent for the α-methylation of alkoxyaryl ketones.
DefinitionChEBI: Methyllithium is an alkyllithium compound and a one-carbon compound.
PreparationMethyllithium is produced industrially by the reaction of methyl chloride or methyl bromide with lithium metal dispersion in diethyl ether. The reaction with methyl chloride yields a solution of methyllithium and a precipitate of lithium chloride which may be readily separated. When methyl bromide is used, the lithium bromide byproduct remains in solution and complexes with the methyllithium. This reduces the reactivity of the methyllithium and, in certain cases, affects its usefulness. On the other hand, the less reactive complex is more stable in diethyl ether. Methyllithium produced from methyl chloride contains only about 0.3 % lithium chloride in a 5 % solution in diethyl ether. It is more reactive than the lithium bromide complex, but decomposes at the rate of 1 % of the contained methyllithium per year (that is 5.00 % solution goes to 4.95 %) at room temperature. The decomposition by ether cleavage results in methane and ethylene formation which increases the pressure in the container on long storage. Methyllithium can be prepared easily in tetrahydrofuran but it has a half-life of only about 2 days at room temperature due to solvent cleavage.
ApplicationMethyllithium solution (1.6M in diethyl ether) has been used for the asymmetric allylic alkylation (AAA) of allylic electrophiles in the presence of a chiral copper catalyst. This protocol leads to the C-C bond formation of tertiary and quaternary stereogenic centers with high enantioselectivity. It can also be used for the synthesis of (?)-salsolidine by reacting with 6,7-dimethoxy-3,4-dihydroisoquinoline in the presence of (?)-sparteine as a chiral ligand.
HazardFlammable, dangerous fire and explosionrisk, self-ignites in air.

Packing &shipping&Payment

Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
Quantity(Kilograms)1 - 10000>10000
Est. Time(days)5To be negotiated

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Article illustrationCompany information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.

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